Single Silver Research Articles

Screen-printing high/low resistance using only a single silver nanowire ink: Resistance-gradient metasurface application for broadband microwave absorption and optical transparency

Transparent metasurface absorbers are highly sought after for their diverse applications, but achieving broad absorption bandwidths without sacrificing optical transparency remains a challenge. Traditionally, enhancing absorption involves increasing substrate thickness, which reduces transmittance. We address this by introducing a resistance-gradient metasurface (RGM) that combines broad absorption with high optical transparency. Unlike conventional methods requiring various inks for different resistances, our approach uses a single silver nanowire ink and screen-printing to create multiple resistances. This technique allows for flexible design and multiple resonances within the metasurface, achieving broad absorption even with a thin substrate. The RGM demonstrates an absorption bandwidth from 8.68 to 11.48 GHz with a substrate thickness of just 0.045 λ0, and optical transmittance of 66.3 % at 550 nm. This innovation promises to enhance both substrate efficiency and bandwidth in transparent metasurface absorbers, broadening their application potential in advanced devices.

Optical resonant cavities carving pathways in tunable wavelength sensitive visible-NIR organic photodetectors

Enhancing the photodetection capabilities of organic photodetectors (OPDs) is crucial for advancing applications in medical monitoring, optical communications, image sensing, and robotics, where a strong, focused peak response at a specific designed wavelength is essential for improving sensitivity, wavelength selectivity, and resolution in imaging systems. By controlled integration of ZnO layers within PBDBT:BTP-4F-based OPDs to form a Fabry-Pérot optical cavity, we developed a cost-effective approach to fabricating highly sensitive OPDs by utilizing PBDBT:BTP-4F organic bulk heterojunctions, and extended its detection wavelengths into the near-infrared (NIR) range. Our design integrates a single silver (Ag) layer that significantly enhances peak detection at a wavelength of 830 ​nm, resulting in a remarkably narrow full-width at half maximum (FWHM) wavelength of 30 ​nm and yielding a photoresponse ten times greater than that of non-resonant devices. Furthermore, by varying the thickness of the ZnO layer from 77 ​nm to 620 ​nm, we achieve high spectral tunability, allowing fine adjustments of the resonant peak across a spectrum ranging from ultraviolet (UV) and visible to NIR wavelengths. This sensitive photodetector is also well-suited for applications in photoplethysmography (PPG), effectively detecting pulse signals in the NIR spectrum which has significant potential in medical diagnostics. This work advances the integration of cost-effective, wavelength-selective spectroscopic visible-NIR OPDs, paving the way for the next generation of sensitive photodetectors.

GLP-1, GIP, and Glucagon Agonists for Obesity Treatment: A Hunger Perspective.

For centuries, increasingly sophisticated methods and approaches have been brought to bear to promote weight loss. Second only to the Holy Grail of research on aging, the idea of finding a single and simple way to lose weight has long preoccupied the minds of laymen and scientists alike. The effects of obesity are far-reaching and not to be minimized; the need for more effective treatments is obvious. Is there a single silver bullet that addresses this issue without effort on the part of the individual? The answer to this question has been one of the most elusive and sought-after in modern history. Now and then, a miraculous discovery propagates the illusion that a simple solution is possible. Now there are designer drugs that seem to accomplish the task: we can lose weight without effort using mono, dual, and triple agonists of receptors for glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), and glucagon. There are, however, fundamental biological principles that raise intriguing questions about these therapies beyond the currently reported side-effects. This perspective reflects upon these issues from the angle of complex goal-oriented behaviors, and systemic and cellular metabolism associated with satiety and hunger.

Efficiently shape-selective synthesis of single crystal silver nanocube with the combination of HNO3/NaCl and reaction time for developing surface enhanced Raman scattering (SERS) substrate

Shape control of noble nanomaterials has garnered significant attention in the past decade because niche applications rely on the relationship between the nanoparticle morphology and optical properties. Although many chemical methods have been reported, there is still a need for improvement in terms of uniformity, yields, and synthesis scale. This work exploited the novel modification approach based on the polyol method to control synthesis to obtain a high amount of single-crystal silver nanocubes (AgNCs) with relatively homogeneous sizes and edge lengths of approximately 100 nm. Furthermore, we have discovered the high effectiveness of controlling temperature conditions to examine the conversion from silver nanocubes to tetrahedron nanoparticles, which had been rarely studied before. These as-prepared AgNCs colloidal solutions were further used to develop the SERS substrate on the glass slide through the facile drop cast method. Additionally, through synthesis using ethylene glycol and redispersed in the ethanol solvent, the obtained AgNCs have a high probability coverage on the glass slide once natural evaporation technique to achieve a remarkable amplification effect and reproducibility behavior. It was explored that these substrates could significantly enhance the Raman signal of 4-mercaptobenzoic acid (4-MBA), which is utilized as the probe molecule to assess the SERS behaviors. The enhancement factor (EF) of the SERS substrates prepared using AgNCs was approximately 3.6 × 106. The presence of 4-MBA could be detected with AgNCs in concentrations ranging from 0.01 to 10 mM, with a limit of detection (LOD) of 8.40 μM and a limit of quantification (LOQ) of 25.46 μM. Through analyzing over 20 different spots on various AgNC substrates, synthesized with similar methods and conditions, the Raman signals of 4-MBA were almost unchanged, with a relative standard deviation (RSD) value of 5.81%, indicating that the SERS signal produced by AgNC substrates was highly reproducible. Based on the results, the SERS nanosubstrates developed with AgNCs could potentially be used to detect trace amounts of other harmful organic compounds.

Influence of Particle Size on Mass Transport during the Oxygen Reduction Reaction at Single Silver Particles Using Scanning Electrochemical Cell Microscopy.

Single entity electrochemical measurements enable insight into the electrocatalytic activity of individual particles based on composition, shape, and crystallographic orientation. In addition to structural effects, particle size can further influence electrocatalytic activity and reaction mechanisms through mass transport effects. In this work, electrodeposition was used to grow well-separated silver particles of varying sizes from 100 to 500 nm in radius. Using a multimicroscopy approach of scanning electrochemical cell microscopy combined with scanning electron microscopy, the electrocatalytic current of individual silver particles toward the oxygen reduction reaction was evaluated as a function of their size. It was found that the current density increased with decreasing particle radius, which was correlated to the mass transport of oxygen to the silver particle, demonstrating the importance of size dependent mass transport effects that can occur at the single particle level using scanning electrochemical cell microscopy and opening new opportunities for quantitative electrocatalysis measurements.

Effect of nano-metallic coating on the wetting of silicon by molten tin at 800 °C

The effects of different nano-metal coatings on the wettability of liquid tin on monocrystalline silicon at 800 °C were discussed, aiming at optimizing the metal bonding technology in high-density chip packaging. Nanometal coatings with different combinations, including silver (Ag), titanium (Ti) and their layered coatings (Ag + Ti), were deposited on monocrystalline silicon by magnetron sputtering, and comparative experiments were carried out. The experimental results show that the metal coating with a thickness of tens of nanometers is enough to completely change the wettability of the system. The improvement of wettability does not follow the idea of active brazing, i.e., there is no need to introduce interfacial active element titanium, and better wettability can be obtained. In the wetting of tin and monocrystalline silicon coated with Ag/Ti or Ti/Ag layered coating, the solid/liquid interface near the triple line forms “pyramid” microstructures, which play a “pinning” role on the triple line. The wettability of monocrystalline silicon coated with a single silver coating with a thickness of 80 nm cannot be significantly improved, and the final wettability is equivalent to the intrinsic wettability of the Sn/Si system (contact angle of 61.2°). When the coating thickness is 160 nm, due to the enrichment of silver at the solid/liquid interface, the locally dissolved silicon precipitates and crystallizes, so that the area of the solid/liquid interface increases, and the triple line cannot be withdrawn. The research results will provide ideas for the optimization and design of metal-substrate bonding in high-density chip packaging.

Unlocking Single Particle Anisotropy in Real‐Time for Photoelectrochemistry Processes at the Nanoscale

AbstractThe key to rationally and rapidly designing high‐performance materials is the monitoring and comprehension of dynamic processes within individual particles in real‐time, particularly to gain insight into the anisotropy of nanoparticles. The intrinsic property of nanoparticles typically varies from one crystal facet to the next under realistic working conditions. Here, we introduce the operando collision electrochemistry to resolve the single silver nanoprisms (Ag NPs) anisotropy in photoelectrochemistry. We directly identify the effect of anisotropy on the plasmonic‐assisted electrochemistry at the single NP/electrolyte interface. The statistical collision frequency shows that heterogeneous diffusion coefficients among crystal facets facilitate Ag NPs to undergo direction‐dependent mass transfer toward the gold ultramicroelectrode. Subsequently, the current amplitudes of transient events indicate that the anisotropy enables variations in dynamic interfacial electron transfer behaviors during photothermal processes. The results presented here demonstrate that the measurement precision of collision electrochemistry can be extended to the sub‐nanoparticle level, highlighting the potential for high‐throughput material screening with comprehensive kinetics information at the nanoscale.

Unlocking Single Particle Anisotropy in Real-Time for Photoelectrochemistry Processes at the Nanoscale.

The key to rationally and rapidly designing high-performance materials is the monitoring and comprehension of dynamic processes within individual particles in real-time, particularly to gain insight into the anisotropy of nanoparticles. The intrinsic property of nanoparticles typically varies from one crystal facet to the next under realistic working conditions. Here, we introduce the operando collision electrochemistry to resolve the single silver nanoprisms (Ag NPs) anisotropy in photoelectrochemistry. We directly identify the effect of anisotropy on the plasmonic-assisted electrochemistry at the single NP/electrolyte interface. The statistical collision frequency shows that heterogeneous diffusion coefficients among crystal facets facilitate Ag NPs to undergo direction-dependent mass transfer toward the gold ultramicroelectrode. Subsequently, the current amplitudes of transient events indicate that the anisotropy enables variations in dynamic interfacial electron transfer behaviors during photothermal processes. The results presented here demonstrate that the measurement precision of collision electrochemistry can be extended to the sub-nanoparticle level, highlighting the potential for high-throughput material screening with comprehensive kinetics information at the nanoscale.

Simultaneous sterilization and biosensing of pathogenic bacteria via copper phthalocyanine-based COF embedded with Cu-N4 single atomic sites and silver nanoparticles

The efficient inactivation and sensitive detection of waste water and food stuffs polluted by pathogenic bacteria are vital for ensuring food safety and protecting people’s healthy. Herein, a 2D copper phthalocyanine-based covalent-organic framework (COF) embraced with Cu-N4 single atomic sites and silver nanoparticles (denoted as CuPc-Dha-COF@AgNPs) was employed as a bifunctional bioplatform for the efficient sterilization via the multi-modal antibacterial mechanism and the sensitive detection of pathogenic bacteria via the photocatalytic oxidization of glutathione (GSH) using a photoelectrochemical (PEC) technique. Given the superior photothermal conversion efficiency, the high production efficiency of reactive oxygen species, the enhanced H2O2 self-supplying capability, and the controlled release of Ag+ ions under near-infrared light irradiation (808 nm and 1.0 W cm−2), 100 % bacteria were eliminated by CuPc-Dha-COF@AgNPs (200 μg mL−1) at 24 h. Furthermore, the CuPc-Dha-COF@AgNPs-based PEC biosensing platform exhibited highly selective determination ability toward GSH because of its superior mimetic enzyme performance caused by Cu-N4 single atomic sites, narrow bandgap, wide photoabsorption performance, and high separation of photoinduced electrons and holes. It thus showed an ultralow detection limit of 99 fM toward GSH within wide range from 1.0 pM to 1.0 nM, as well as high selectivity, good stability and reproducibility, and promising practicality. This work provides a new strategy for the sterilization and sensitive detection of pathogenic bacteria, simultaneously implementing and monitoring measures for the water system and food safety.

Low-cost, reliable and flexible piezoresistive pressure sensors coated with single layer graphene and silver nanowires on three-dimensional polyurethane sponge

Flexible wearable sensors perform a significant role in practical applications such as medical monitoring, rehabilitation exercises, and artificial skin, as they can quantify and visualize external stress and strain. Polyurethane (PU) sponge stands out as a highly elastic and reproducible material frequently employed as a substrate in flexible electronic devices. Sponge materials with different pore sizes and densities exhibit varying degrees of deformation resistance under long-term cyclic pressure, thereby affecting the performance of sensors. Herein, piezoresistive pressure sensors based on PU with different pore diameters were successfully fabricated by dip-coating technology. By incorporating silver nanowires (AgNWs) and single layer graphene (SLG) into the sponge, both the low-density and high-density composite sponges can withstand over 70 % compressive strain, with stresses of 62.57 kPa and 31.79 kPa, respectively. Moreover, high-density composite sponge demonstrates a more stable conductive structure, more consistent relative resistance and better flame-retardant performance. The response and recovery time between 10 % and 40 % strains of the resulting pressure sensor based on high-density composite sponge (PU@AgNWs@SLG) are 110 ms and 106 ms and its gauge factor reaches 2.39. The pressure sensor exhibits a satisfactory reproducibility after over 3000 compression-release cycles, and performs during various applications, such as controlling brightness of LEDs, monitoring human activities, sensing finger movements.

Highly efficient electric-thermal conversion of Silver/PVP composites for micro initiators by direct ink writing

Traditional film initiator fabrication techniques were limited by material and process constraints, resulting in restricted ignition capability, durability issues, and complexity in manufacturing. In this study, Metal/polymer composite materials were applied in film initiators in order to enhance the mechanical properties, longevity, and thermal attributes. Silver/polyvinylpyrrolidone composite film bridge (SPB) initiators were fabricated by direct ink writing (DIW). By adjusting the silver loading level and sintering temperature in the Ag nanoparticles/polyvinylpyrrolidone (Ag NPs/PVP) ink formulation, precise control over the structure and resistivity of the SPB was achieved. Compared to single silver film bridge (SFB) initiators prepared by magnetron sputtering (MS), SPBs demonstrated superior heating performance, higher current carrying capacity, and energy utilization under constant current excitation. In capacitor discharge tests, SPBs exhibited superior electric explosion characteristics and plasma properties, with a 25.53% higher energy utilization efficiency compared to SFBs. The peak plasma electron temperature of SPBs reached 7610 K, which was 1065 K higher than that of SFBs. This makes Silver/polyvinylpyrrolidone composite highly promising practical alternatives for high-efficiency, stable, and reliable ignition processes, with potential widespread applications in the aerospace field.

Localized surface plasmon resonance (LSPR) excitation on single silver nanoring with nanoscale surface roughness

With the expansion of the application of high-sensitivity Surface-enhanced Raman scattering (SERS) technique, micro SERS-active substrates with rich optical properties and high-level functions are desired. In this study, silver nanorings with nanoscale surface roughness were fabricated as a new type of enclosed quasi-2D micro-SERS-active substrate. Highly-crystalline spherical and hemispherical silver nanoprotrusions were densely and uniformly distributed over the entire surface of the nanorings. The SERS signals were significantly enhanced on the roughened silver nanorings which were mainly derived from the maximal localized surface plasmon resonance (LSPR) points at the junctions between adjacent coupled nanoprotrusions on the roughened nanorings. The mapping image shows a uniform and intense LSPR enhancement over the nanorings, owing to the uniform and dense distribution of silver nanoprotrusions and the resulting uniform distribution of maximal LSPR points on the roughened nanorings. The dark-field spectra further indicated that the single roughened silver nanoring had significant LSPR enhancement, a wide LSPR frequency-range response, and adaptability for SERS enhancement. Notably, both the measured and simulated results demonstrate that the maximal LSPR enhancement at the junctions between the nanoprotrusions, which are distributed on the inner surface of the silver nanoring, is higher than that on the outer surface because of the plasmon-focusing effect of the enclosed silver nanoring, which leads to the lateral asymmetrical distribution of LSPR intensity, indicating more LSPR and SERS features. These results indicate that single roughened silver nanorings exhibit excellent performance as a new type of enclosed quasi-2D silver nanoring micro-SERS-active substrate, microzone LSPR catalysis, and micro/nanodevices.

Single Atom-Dispersed Silver Incorporated in ZIF-8-Derived Porous Carbon for Enhanced Photothermal Activity and Antibacterial Activities.

Recently, Single-atom-loaded carbon-based material is a new environmentally friendly and stable photothermal antibacterial nanomaterial. It is still a great challenge to achieve single-atom loading on carbon materials. Herein, We doped single-atom Ag into ZIF-8-derived porous carbon to obtain Ag-doped ZIF-8-derived porous carbon(AgSA-ZDPC). The as-prepared samples were characterized by XRD, XPS, FESEM, EDX, TEM, and HAADF-STEM which confirmed that the single-atom Ag successfully doped into the porous carbon. Further, the photothermal properties and antimicrobial activity of AgSA-ZDPC have been tested. The results showed that the temperature increased by 30 °C after near-infrared light irradiation(1 W/cm2) for 5 min which was better than ZIF-8-derived porous carbon(ZDPC). It also exhibits excellent photothermal stability after the laser was switched on and off 5 times. When the AgSA-ZDPC concentration was greater than 50 µg/mL and the near-infrared irradiation was performed for 5 min, the growth inhibition of S. aureus and E. coli was almost 100%. This work provides a simple method for the preparation of single-atom Ag-doped microporous carbon which has potential antibacterial application.

Improving the Uniformity of Top Emitting Organic Light Emitting Diodes Using a Hybrid Electrode Structure

AbstractSome applications of organic light‐emitting diodes (OLEDs) require large area, high light output, and high uniformity. It is difficult to achieve these attributes simultaneously because of voltage drops in the contacts, which cannot easily satisfy high optical transparency and electrical conductivity simultaneously. In large area OLEDs, thin electrodes with high sheet resistance induce voltage drops across the devices, leading to non‐uniform distribution of light. However, thick electrodes with low sheet resistance decrease the light output due to low transmittance. To overcome this trade‐off, a multilayer hybrid electrode based on Ag (20 nm)/WO3/Ag (20 nm)/WO3 is designed to obtain high electrical conductance with low optical loss. Compared to conventional devices using a single Ag (40 nm) top electrode, there is a considerable increase in the external quantum efficiency (EQE) of the device using this electrode (from 11.5% to 25.5% at 1000 cd m−2), while maintaining similar sheet resistance. In addition, a large area (≈57 cm2) OLED with the hybrid electrode demonstrates a luminance uniformity of 77% as compared to a device using single silver electrode with uniformity of 66%. Therefore, the proposed Ag/WO3/Ag/WO3 hybrid electrode is a promising choice for the fabrication of efficient and uniform large‐area OLEDs.

Evaluation of low-emissivity coatings with single, double, and triple silver layers

In this work, a detailed study is conducted on the visible transmittance, solar reflectance, and emissivity properties of low-emissivity coatings composed of one, two, and three layers of silver. The results demonstrate significant enhancements in both optical and thermal properties achievable by increasing the number of silver layers, leading to coatings that are more transparent in the visible spectrum, more reflective in the near-infrared, with lower emissivity and lower sheet resistance. The aesthetic adjustment possibilities of the different structures are also examined, with coatings composed of three layers of silver being more flexible.

Experimental Investigation on Laser-Induced Electrochemical Silver Plating Technology.

The silver coating is widely used in electronic device manufacturing due to its excellent conductivity and soldering properties. Conventional preparation of local silver coating often uses the preplated silver, mask high-speed silver plating, and deplated silver processes. In this paper, the laser-induced electrodeposition technique is used to perform maskless laser-induced localized electrodeposition on a copper substrate preplated with a layer of silver. After the deplated silver process, ultrathin silver coatings with high dimensional accuracy, good corrosion resistance, and good bonding were obtained. The spatial distribution of the transient temperature field under laser irradiation is studied, the variation pattern of cathode substrate current under laser irradiation is tested, and finally, the spatial distribution of the pressure field under laser irradiation is simulated by Comsol. The effect of different laser scanning methods on the coating morphology was investigated, and the experimental study of the different single pulse energy-induced localized silver coatings was systematically carried out. The results show that the localized coating obtained by cross-line scanning with a laser single pulse energy of 93 μJ is flat with a film thickness of 0.23 μm, high dimensional accuracy, and good bonding force and corrosion resistance properties. This method provides a new approach for the preparation of a localized silver coating.

Green synthesis of silver nanoparticles using Mentha crispa L. leaf extract for treatment of dye wastewater

Mentha crispa L. is one of Vietnam’s most precious folk medicines and is also a spice used in many delicious dishes in Vietnam and around the world. The use of Mentha crispa L. leaf extract as a reducing agent for Ag+ ions to synthesize silver nanoparticles is discussed in this paper. Single silver nanospheres were dispersed in biological media and their sizes were controlled in the range of 20-80 nm. Factors affecting particle size and shape such as extract concentration, AgNO3 concentration, reaction time, and temperature were investigated to determine the optimal parameters for particle synthesis. The optical properties, dispersion, crystal structure, morphology, and sizes of silver nanoparticles were investigated through UV-Vis absorption spectroscopy, dynamic light scattering (DLS) measurements, X-ray diffraction, and transmission electron microscopy (TEM). The functional groups on the L.AgNPs were determined by Fourier-transform infrared (FTIR) transmittance spectra. The synthesised silver nanoparticles were used to treat methylene blue (MB) dye, the main component of dye wastewater, based on their photocatalytic properties. The results show that in the presence of L.AgNPs, the photodegradation efficiency of NaBH4 or H2O2 reducing agents is much higher, up to 95% of illumination.

Resonance Light-Scattering Correlation Spectroscopy and Its Application in Analytical Chemistry for Life Science.

Resonance light-scattering correlation spectroscopy (RLSCS) is a new single-particle detection method with its working principle being like fluorescence correlation spectroscopy (FCS). RLSCS is obtained by autocorrelation function analysis on the measured fluctuation of the resonance light scattering (RLS) intensity occurring within a subfemtoliter volume when a single nanoparticle (such as gold nanoparticles (NPs) or silver (SNPs)) freely diffuses through the volume. The RLSCS technique can detect such parameters as concentration, diffusion coefficient (translation and rotation), etc. Compared with the FCS technique, the correlated fluorescence intensity signal in RLSCS is replaced with the RLS signal of the nanoparticles, overcoming some limits of the fluorescent probes such as photobleaching under high-intensity or long-term illumination. In this Account, we showcase RLSCS methods, theoretical models at different optical configurations, and some key applications. First, the RLSCS optical detection system was constructed based on the confocal optics, its theoretical model was proposed, and the diffusion behaviors of the nanoparticles in the solution were studied including the rotational and translational diffusion. And, methods were developed to measure the concentration, size, aspect ratio, and size distribution of the NPs. Second, based on the RLSCS methods, some detection strategies were developed for homogeneous DNA detection, immunoassay, apoptosis assay, self-thermophoresis of the nanomotor, and quantitative assay in single living cells. Meanwhile, a new fluorescence/scattering cross-correlation spectroscopy (FSCCS) method was proposed for monitoring the molecule-particle interaction. This method enriched the conventional fluorescence/fluorescence cross-correlation spectroscopy (FCCS) method. Third, using the EMCCD with high sensitivity and rapid response as an optical detector, two temporospatially resolved scattering correlation spectroscopy methods and their theoretical models were developed: total internal reflection (TIR) configuration-based spatially resolved scattering correlation spectroscopy (SRSCS) and dark-field illumination-based scattering correlation spectroscopy (DFSCS). These methods extended single-spot confocal RLSCS to imaging RLSCS, which makes RLSCS have the ability for multiple channel detection with temporospatial resolution. The method was successfully used for investigating the dynamic behaviors of gold NPs in live cells and obtained its temporospatial concentration distribution and diffusion behaviors. The final section of this Account outlines future directions in the development of RLSCS.

High-efficient Ag(I) ion binding, Ag(0) nanoparticle loading, and iodine trapping in ultrastable benzimidazole-linked polymers

Interest in functional silver has rapidly grown over the years due to significant advances in separation, sensing, catalysis, and biomedical applications. Here we developed a new strategy to load single atomic silver species in the rigid and open unit of the fully conjugated benzimidazole-linked polymers (BILPs). Due to the well-defined chelating units of N-heterocycles, the Ag+ ion species can be coordinated by N ligands and stabilized in the atomic level without aggregating into nanoscale Ag clusters and nanoparticles. The obtained Ag+-BILP-101 exhibits a selective binding property of Ag+ ions from solutions. The ultrastable structure and the property of taking up metal species, endow BILPs with the advantages of functionalizing metal species. After the reduction by NaBH4, the Ag+ ions were transferred into Ag nanoparticles. The substantial and intrinsic porosity of BILPs also gives excellent accessibility to Ag species loaded in the frameworks. The plentiful N-heterocycles and loaded Ag species show a synergistic/coadsorption effect for iodine vapor, and the charge transfer from frameworks promotes the formation of iodide ions. The iodine capture capacities of Ag+-BILP-101 and Ag0-BILP-101 reach 3.3 g/g and 3.7 g/g at 80 ℃, and still maintain 3.2 g/g and 3.5 g/g at 150 ℃, respectively. After ethanol elution, the residual iodine/Ag molar ratios in Ag+/Ag0-BILP-101 samples are still more than one (about 1.5), suggesting their strong affinity toward iodine. This work highlights the excellent selective Ag+ ion binding and Ag species supporting properties of BILPs, which can extend to other porous organic framework platforms for various applications based on silver species-skeleton interactions.

Dynamic imaging of interfacial electrochemistry on single Ag nanowires by azimuth-modulated plasmonic scattering interferometry

Direct visualization of surface chemical dynamics in solution is essential for understanding the mechanisms involved in nanocatalysis and electrochemistry; however, it is challenging to achieve high spatial and temporal resolution. Here, we present an azimuth-modulated plasmonic imaging technique capable of imaging dynamic interfacial changes. The method avoids strong interference from reflected light and consequently eliminates the parabolic-like interferometric patterns in the images, allowing for a 67-fold increase in the spatial resolution of plasmonic imaging. We demonstrate that this optical imaging approach enables comprehensive analyses of surface chemical dynamics and identification of previously unknown surface reaction heterogeneity by investigating electrochemical redox reactions over single silver nanowires as an example. This work provides a general strategy for high-resolution plasmonic imaging of surface electrochemical dynamics and other interfacial chemical reactions, complementing existing surface characterization methods.